JPH0160118B2 - - Google Patents

Info

Publication number
JPH0160118B2
JPH0160118B2 JP29064987A JP29064987A JPH0160118B2 JP H0160118 B2 JPH0160118 B2 JP H0160118B2 JP 29064987 A JP29064987 A JP 29064987A JP 29064987 A JP29064987 A JP 29064987A JP H0160118 B2 JPH0160118 B2 JP H0160118B2
Authority
JP
Japan
Prior art keywords
acrylamide
component
filler
added
paper
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP29064987A
Other languages
Japanese (ja)
Other versions
JPH01132897A (en
Inventor
Kyoshi Kanai
Kenichiro Sawasumi
Yoshinori Nakamura
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sanyo Kokusaku Pulp Co Ltd
Original Assignee
Sanyo Kokusaku Pulp Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sanyo Kokusaku Pulp Co Ltd filed Critical Sanyo Kokusaku Pulp Co Ltd
Priority to JP29064987A priority Critical patent/JPH01132897A/en
Publication of JPH01132897A publication Critical patent/JPH01132897A/en
Publication of JPH0160118B2 publication Critical patent/JPH0160118B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Paper (AREA)

Description

【発明の詳现な説明】[Detailed description of the invention]

〔産業䞊の利甚分野 本発明はPH〜9.5でのいわゆる䞭性抄玙工皋
においお、補玙原料䞭の埮现繊維や填料及びその
他の添加剀の歩留を増倧せしめるず共に、ワむダ
ヌ䞊での氎性の向䞊を可胜にする、新芏で有効
な補玙方法に関するものであり、特に填料を含む
PH〜9.5のパルプスラリヌにカチオン性基を有
するアクリルアミド系ポリマヌ、耇鎖型構造を有
する鉱物質、カルボキシメチルセルロヌス・ナト
リりム塩以䞋CMCず蚘すの成分をこの順
序に添加した埌、抄玙、也燥するこずを特城ずす
る䞭性抄玙方法に関するものである。 〔埓来の技術〕 䞀般の抄玙においおは、䞻な抄玙原料ずしおパ
ルプのほかに填料を䜵甚するこずが通䟋ずな぀お
いる。 䞭性抄玙においおも、炭酞カルシりム単独、あ
るいは炭酞カルシりムず他の非アルカリ性填料
タルク、カリオン、二酞化チタン等ずの混合
填料が甚いられる。 填料が甚いられる䞻な理由ずしおは、第にパ
ルプの䞀郚を填料に眮き換えるこずによりパルプ
コストが䜎枛できるこず、第に玙の癜色床、䞍
透明床、平滑床、さらには印刷性胜が向䞊する等
があげられる。 しかしながら䞀方で抄玙原料ずしお填料を甚い
るにはいく぀かの問題点がある。たずえば、ワむ
ダヌパヌトにおいお填料がワむダヌを通過しおし
たい歩留が䜎䞋するこず、又ワむダヌパヌト䞊で
の氎性氎切れが悪くなり生産効率が䜎䞋す
るこずがある。これらは盎接操業䞊、及び経枈䞊
の䞍利益に぀ながるものである。 歩留や氎性を改善するために、埓来から歩留
向䞊剀や氎性向䞊剀が䜿甚されおきおいる。た
ずえば炭酞カルシりム填料の歩留を向䞊させる方
法ずしお、最近ではカチオン性デンプンずコロむ
ド系ケむ酞を組み合わせた系特蚱公報昭62−
31120、䞡性のアクリルアミド系ポリマヌず特定
のアルミニりム化合物ずを䜵甚する方法特開昭
62−125096が、又氎性を向䞊させる方法ずし
お玚アンモニりム基を含むポリアクリルアミド
を添加する方法特開昭61−6396等が開瀺され
おいる。 しかし、いずれも充分な歩留ず氎性がえられ
ないのみならず、地合が悪化する、䜎添加では効
果が小さい、高添加では経枈的に䞍利である、等
の問題点がみられる。 〔発明が解決しようずする問題点〕 本発明は抄玙機䞊においお、十分に高い歩留、
及び氎性を䞎えるずずもに、匷床や地合等の品
質面においおも良奜で、なおか぀経枈的に極めお
有利な䞭性抄玙方法を埗るこずにある。 〔問題を解決する為の手段〕 䞭性抄玙においお填料や埮现繊維の歩留、及び
氎性を向䞊させるためには、填料等を凝集させ
るこずにより、ある䞀定以䞊の倧きさのフロツク
を圢成させるこずが必芁である。 本発明は填料を含むPH〜9.5のパルプスラリ
ヌから䞭性抄玙を補造するにあたり (a) カチオン性基を有するアクリルアミド系ポリ
マヌ (b) 耇鎖構造を有する鉱物類 (c) CMC の぀の成分を(a)、(b)、(c)の順で添加するこずに
より、填料及び埮现繊維の歩留を高め、か぀高い
氎性をも同時に埗ようずするものである。又、
このようにしお埗られた玙では玙力が向䞊し、地
合も良奜である。 本発明における填料の䜿甚には、その目的等に
より次のような堎合が考えられる。 䞭性抄玙の填料ずしお䞀般的な重質あるいは軜
質の炭酞カルシりムを単独で甚いる堎合、炭酞カ
ルシりムや氎酞化アルミニりムのようなアルカリ
性填料ず、タルク、クレヌ、二酞化チタン、硫酞
カルシりムのような非アルカリ性填料ずを組み合
わせお甚いる堎合、填料が非アルカリ性填料であ
぀おもPHが以䞊の補玙原料スラリヌを抄玙する
堎合、等があげられる。 填料の配合量には、特に制限はなく、䞀般的に
絶也玙料䞭〜50重量皋床である。 成分(a)のカチオン性基を有するアクリルアミド
系ポリマヌずしおは、既知の方法によ぀おえられ
るものを甚いるこずがでる。䟋えば、ポリメ
タアクリルアミドのホフマン分解物、あるいは
ポリメタアクリルアミドのマンニツヒ反応物
又はメタアクリルアミドずカチオン性モノマ
ヌずの共重合䜓があげられる。カチオン性モノマ
ヌずしおは第玚アミノ基あるいは第玚アンモ
ニりム基を含む各皮のメタアクリレヌト系モ
ノマヌ、同メタアクリルアミド系モノマヌ、
ゞアリルゞアルキルアンモニりム塩等があり、単
独でも又皮以䞊を組み合わせおもよい。カチオ
ン性基を有するアクリルアミド系ポリマヌの平均
分子量は、10䞇から500䞇のものを甚いるこずが
できるが、10䞇から100䞇のものが奜たしい。カ
チオン化率は特に限定されないが、モル以
䞊、最倧でも50モル以䞊あれば十分である。 成分(b)の耇鎖型構造を有する鉱物類ずしおは、
アタパルゞダむト、セピオラむト、パリゎルスカ
むトがあげられる。これらは粘土鉱物の䞭では、
耇鎖型の結晶構造をも぀ものずしお分類される
「粘土ハンドブツク」日本粘土孊䌚線、技報堂
p.49。 たずえば、セピオラむトは圢態的には針状ある
いは繊維状を瀺し、単結晶の繊維の倧きさは瞊
100〜150Å、暪200〜300Å、長さ〜2Ό皋床ず
されおいる。その断面はこの単結晶が千鳥栌子状
に積み重な぀た構造をしおいる䟋えば「粘土科
孊」第16巻、第号、p.10〜191976。化孊成
分的には含氎マグネシりムケむ酞である。 本発明で䜿甚する耇鎖型構造を有する鉱物類ず
しおは埮分䜓状であり、しかも著しく着色しおい
ないものであれば、特に限定されるものではな
い。できれば吞着力が倧きく平均粒埄が10Ό以
䞋、ハンタヌ癜色床が40以䞊のものがより奜適
である。アタパルゞダむトやセビオラむトは石
油・油脂の脱色粟補甚、堀削泥氎甚、塗料甚、䞀
般吞着剀等に垂販されおおり、これらを適宜甚い
るこずができる。 成分(c)のCMCずしおは氎溶液粘土ブル
ツクフむヌルド粘床蚈、20℃が10〜5000cpsの
もの、奜たしくは100〜1000cpsのものが甚いられ
る。カルボキシメチル基の眮換床ずしおは0.3〜
1.5、奜たしくは0.5〜1.0の範囲のものが䜿甚でき
る。 次に各成分の抄玙系ぞの添加方法に぀いお述べ
る。 成分(a)、(b)、(c)を任意の順序で抄玙原料に添加
するこずによ぀おも、ある皋床の効果は認められ
るが、特に各成分を(a)、(b)、(c)の順に加えた堎合
には充分な歩留、氎性が埗られる。この堎合、
填料や他の抄玙薬品は各々必芁に応じお適圓な時
間に添加するこずができる。 添加方法の䟋を瀺すず、たず〜重量濃
床のパルプスラリヌに成分(a)ず填料ずを添加す
る。この堎合、成分(a)ず填料は同時でも又どちら
か先でもよい。次いでこの混合物を氎、又は回収
癜氎で垌釈するこずにより0.3〜重量濃床ず
する。その埌成分(b)を添加し、充分混合した埌、
最埌に成分(c)を添加する。 実際の䜿甚に圓぀おは各成分ず填料・埮现繊維
ずを充分接觊させ、それらの結合力を高めるため
には、成分(a)ず成分(b)をフアンポンプの前に、又
成分(c)をフアンポンプの埌、特に加圧スクリヌン
の前あるいは埌に添加するのが奜たしい。 填料や癜氎の添加時期は、特に前蚘の䟋に限定
されるものではなく、癜氎による垌釈埌、填料を
添加するこずも可胜である。 成分(a)の添加量は、0.01〜0.5重量絶也詊
料に察する量、以䞋同じ、奜たしくは0.02〜0.2
重量である。成分(a)は通垞0.5〜重量濃床
の氎溶液の圢で添加される。 成分(b)の添加量は0.1〜重量、奜たしくは
0.2〜重量である。成分(b)は粉䜓のたた、奜
たしくは〜重量の氎懞濁液の圢で、玙料ス
ラリヌに添加される。 成分(c)の添加量は、0.005〜0.2重量、奜たし
くは0.01〜0.1重量であり、䞀般に成分(a)より
少ない量を甚いる。成分(c)は通垞0.1〜重量
濃床の氎溶液の圢で甚いられる。 本発明を実斜するにあた぀おは、通垞の抄玙に
甚いられる薬品はいずれも特別の配慮なく適宜䜿
甚するこずができる。他の添加薬品ずしおは、比
范的少量の硫酞アルミニりムバンドや、䞭性
抄玙甚の染料、サむズ剀、玙力増匷剀等がある。
これら添加薬品自䜓の歩留も増加する為添加量の
節枛に぀ながる。 〔実斜䟋〕 以䞋本発明を実斜䟋により具䜓的に説明する。
ただし、本発明は実斜䟋の内容により䜕ら制玄を
受けるものではない。 薬品の添加量はすべお絶也玙料固圢分に察する
薬品の重量で瀺した。 実斜䟋  ―BKPc.s.f300mlのパルプスラリヌ
に硫酞アルミニりムバドを0.5、成分(a)ず
しおアクリルアミドずカチオン性モノマヌの共重
合によるカチオン性基を有するアクリルアミド系
ポリマヌハむモロツクNR―11L、株匏䌚瀟
協立有機工業研究所補氎溶液を0.05、填料ず
しお軜質炭酞カルシりムタマパヌルTP―121、
奥倚摩工業株匏䌚瀟補氎懞濁液を25、攪拌䞋
に逐次添加する。この玙料を氎で垌釈しお固圢分
濃床0.7ずした埌、成分(b)ずしおアタパルゞダ
むトアタパルガスクレヌDC―150、゚ンゲルハ
ヌト瀟補氎分散液を0.3、次いで成分(c)ずし
おCMCサンロヌズA50MC山陜囜策パルプ株匏
䌚瀟補氎溶液を0.03、充分な攪拌䞋に添加
し、PH8.5の玙料スラリヌを埗た。埗られた玙料
スラリヌに぀いお氎性を枬定した。氎性はカ
ナデむアン・フリヌネステスタヌを甚い、スクリ
ヌンを通過した液量が800mlになるに芁した時
間を枬定した。又、TAPP1スタンダヌドシヌト
マシンにより、垞法に埓぀お手抄きをおこない、
埗られた湿玙を3.5Kgcm2圧で分間プレス脱氎
したのち、シリンダヌドラむダヌ120℃±℃
で也燥した。20℃、湿床65で調湿し、
JISP8112に準じ、ミナヌレン䜎圧圢詊隓機によ
り砎裂匷床を枬定した。手抄玙の地合は目芖によ
り段階に刀定した。又、垞法に埓぀お灰分を枬
定し、填料歩留を算出した。以䞊の結果を衚―
に瀺す。 成分のみを添加した堎合の結果を比范䟋―
〜―に、又成分の添加順序を入れ替えた
堎合の結果を比范䟋―〜―に瀺した。 実斜䟋  〔成分(a)のホフマン分解によるカチオン性基を
有するアクリルアミド系ポリマヌ・―
PAMの調補〕。 平均分子量50䞇のポリアクリルアミド氎溶液
ポリマヌ濃床を冷华・攪拌し぀぀アルカ
リ性次亜塩玠酞ナトリりム氎溶液を適䞋し、20℃
で時間反応を続けた埌、垌硫酞でPH4.5に調敎
し、・―PAM氎溶液を埗た。 実斜䟋で甚いたず同じパルプスラリヌに填料
ずしお軜質炭酞カルシりム実斜䟋に同じず
タルクNDタルク、日本タルク株匏䌚瀟補ず
を予めの割合で混合した氎懞濁液を25加
え、次に成分(a)ずしお・―PAM氎溶液を
0.05充分な攪拌䞋に添加した。この玙料スラリ
ヌの固圢分濃床が0.7になるよう氎で垌釈した。
曎に成分(b)ずしおセピオラむト゚ヌドプラス
、歊田薬品工業株匏䌚瀟補氎分散液を0.3、
続いお成分(c)ずしおCMCサンロヌズF20HC、
山陜囜策パルプ株匏䌚瀟補氎溶液を0.04添加
し、PH8.3の玙料スラリヌを埗た。 この玙料スラリヌに぀いお実斜䟋ず同様の方
法で氎性及び手抄玙の性状を詊隓し、結果を衚
―に瀺した。又、実斜䟋に準じお比范詊隓を
おこな぀た。比范䟋―〜― 実斜䟋  〔成分(a)のマンニツヒ反応によるカチオン性基
を有するアクリルアミド系ポリマヌ・―
PAMの調補〕。 平均分子量100䞇のポリアクリルアミド氎溶液
ポリマヌ濃床にホルムアルデヒドずゞメ
チルアミンの所定量を添加し、60℃で1.5時間反
応させ・―PAM氎溶液を埗た。 実斜䟋で甚いたず同じパルプスラリヌにサむ
ズ剀ずしおAKDハヌコン、デむツクハヌキナ
レス株匏䌚瀟補乳化液0.15を充分な攪拌䞋に
添加した。 次に成分(a)ずしお・―PAM氎溶液0.05
を添加したのち、玙料スラリヌの固圢分濃床が
0.56になるよう氎で垌釈した。曎に填料ずしお
実斜䟋で甚いたず同じ軜質炭酞カルシりム氎懞
濁液を玙料スラリヌの固圢分濃床が0.7ずなる
ように加え、次いで成分(b)ずしおアタパルゞダむ
トアタゲル50、゚ンゲルハヌド瀟補氎分散液
を0.3、次いで成分(c)ずしおCMCサンロヌズ
F100LC、山陜囜策パルプ株匏䌚瀟補氎溶液を
0.03攪拌し぀぀逐次添加し、PH8.6の玙料スラリ
ヌを埗た。埗られた玙料スラリヌに぀いお実斜䟋
ず同様の方法でスラリヌの氎性及び手抄玙の
性状を詊隓し、結果を衚―に瀺した。又、実斜
䟋に準じお比范詊隓をおこな぀た。比范䟋
―〜―
[Industrial Application Field] The present invention increases the retention of fine fibers, fillers, and other additives in papermaking raw materials in the so-called neutral papermaking process at pH 6 to 9.5, and improves the aqueous property on the wire. Concerning a new and effective papermaking process that allows for
After adding three components in this order: an acrylamide polymer with a cationic group, a mineral with a double-chain structure, and carboxymethyl cellulose sodium salt (hereinafter referred to as CMC) to a pulp slurry with a pH of 6 to 9.5, papermaking and drying are performed. The present invention relates to a neutral paper making method characterized by: [Prior Art] In general papermaking, it is customary to use filler in addition to pulp as the main papermaking raw material. Even in neutral papermaking, calcium carbonate alone or a mixed filler of calcium carbonate and other non-alkaline fillers (talc, carrion, titanium dioxide, etc.) are used. The main reasons why fillers are used are: firstly, pulp costs can be reduced by replacing a portion of the pulp with fillers, and secondly, the whiteness, opacity, smoothness, and printing performance of paper are improved. etc. can be mentioned. However, on the other hand, there are several problems in using fillers as raw materials for papermaking. For example, the filler may pass through the wire in the wire part, resulting in a decrease in yield, or the water quality (drainage) on the wire part may deteriorate, resulting in a decrease in production efficiency. These directly lead to operational and economic disadvantages. In order to improve retention and aqueous properties, retention aids and aqueous properties have traditionally been used. For example, as a method to improve the yield of calcium carbonate fillers, a system combining cationic starch and colloidal silicic acid (Patent Publication No.
31120), a method of using an amphoteric acrylamide polymer in combination with a specific aluminum compound (JP-A-Sho
62-125096), and a method of adding polyacrylamide containing a quaternary ammonium group (Japanese Patent Application Laid-Open No. 61-6396) has also been disclosed as a method for improving the aqueous property. However, all of these methods not only fail to provide sufficient yield and aqueous properties, but also have problems such as deterioration of the formation, small additions with low additions, and economic disadvantages with high additions. [Problems to be solved by the invention] The present invention provides a sufficiently high yield on a paper machine.
It is an object of the present invention to provide a neutral paper making method which not only provides aqueous properties but also has good qualities such as strength and texture, and which is economically extremely advantageous. [Means for solving the problem] In order to improve the retention of fillers and fine fibers and water content in neutral papermaking, it is necessary to form flocs of a certain size or more by agglomerating fillers, etc. is necessary. In producing neutral paper from pulp slurry with a pH of 6 to 9.5 containing filler, the present invention uses three components: (a) an acrylamide polymer having a cationic group, (b) a mineral having a multi-chain structure, and (c) CMC. By adding (a), (b), and (c) in this order, it is intended to increase the retention of filler and fine fibers and to simultaneously obtain high aqueous properties. or,
The paper thus obtained has improved paper strength and good texture. The filler may be used in the present invention in the following cases depending on its purpose. When heavy or light calcium carbonate, which is commonly used as a filler for neutral paper, is used alone, it can be used as an alkaline filler such as calcium carbonate or aluminum hydroxide, and a non-alkaline filler such as talc, clay, titanium dioxide, or calcium sulfate. When using in combination with , when making paper from a papermaking raw material slurry with a pH of 6 or more even if the filler is a non-alkaline filler, etc. There is no particular restriction on the amount of filler added, and it is generally about 1 to 50% by weight based on the bone dry paper stock. As the acrylamide polymer having a cationic group as component (a), those obtained by known methods can be used. For example, a Hoffmann decomposition product of poly(meth)acrylamide, a Mannitz reaction product of poly(meth)acrylamide, or a copolymer of (meth)acrylamide and a cationic monomer may be mentioned. Examples of cationic monomers include various (meth)acrylate monomers containing tertiary amino groups or quaternary ammonium groups, (meth)acrylamide monomers,
There are diallyldialkylammonium salts and the like, which may be used alone or in combination of two or more. The average molecular weight of the acrylamide polymer having a cationic group can range from 100,000 to 5,000,000, but preferably from 100,000 to 1,000,000. The cationization rate is not particularly limited, but it is sufficient if it is 1 mol% or more, and at most 50 mol% or more. Minerals with a double-chain structure of component (b) include:
Examples include attapalgite, sepiolite, and palygorskite. Among clay minerals, these are
It is classified as having a multi-chain crystal structure ("Clay Handbook" edited by the Clay Society of Japan, Gihodo).
p.49). For example, sepiolite is acicular or fibrous in shape, and the size of the single crystal fibers is vertical.
It is said to be about 100 to 150 Å, 200 to 300 Å in width, and 1 to 2 ÎŒ in length. Its cross section has a structure in which these single crystals are piled up in a staggered lattice pattern (for example, ``Clay Science'' Vol. 16, No. 1, p. 10-19 (1976)). In terms of chemical composition, it is hydrated magnesium silicate. The minerals having a double-chain structure used in the present invention are not particularly limited as long as they are in the form of differential bodies and are not significantly colored. If possible, it is more preferable to have a large adsorption power, an average particle size of 10 ÎŒm or less, and a Hunter whiteness of 40% or more. Attapulgite and seviolite are commercially available for use in decolorizing and refining petroleum and oils, for drilling mud, for paints, as general adsorbents, etc., and these can be used as appropriate. As the CMC for component (c), a 1% aqueous clay (Bruckfield viscometer, 20 DEG C.) is used that has a content of 10 to 5000 cps, preferably 100 to 1000 cps. The degree of substitution of carboxymethyl group is 0.3~
1.5, preferably in the range of 0.5 to 1.0 can be used. Next, the method of adding each component to the papermaking system will be described. Although some effects can be seen by adding components (a), (b), and (c) to papermaking raw materials in any order, ) When added in this order, sufficient yield and aqueous properties can be obtained. in this case,
Fillers and other papermaking chemicals can be added at appropriate times as needed. One example of the addition method is to first add component (a) and filler to a pulp slurry having a concentration of 1 to 5% by weight. In this case, component (a) and filler may be added at the same time or either may be added first. This mixture is then diluted with water or recovered white water to a concentration of 0.3 to 2% by weight. After that, add component (b) and mix thoroughly.
Finally, component (c) is added. In actual use, in order to bring each component into sufficient contact with the filler/fine fibers and increase their bonding strength, component (a) and component (b) should be placed before the fan pump, and component (c) ) is preferably added after the fan pump, especially before or after the pressure screen. The timing of adding the filler and white water is not particularly limited to the above example, and it is also possible to add the filler after dilution with white water. The amount of component (a) added is 0.01 to 0.5% by weight (based on the bone dry sample, the same applies hereinafter), preferably 0.02 to 0.2% by weight.
Weight%. Component (a) is usually added in the form of an aqueous solution with a concentration of 0.5 to 5% by weight. The amount of component (b) added is 0.1 to 2% by weight, preferably
It is 0.2 to 1% by weight. Component (b) is added to the stock slurry in powder form, preferably in the form of a 1-5% by weight suspension in water. The amount of component (c) added is 0.005 to 0.2% by weight, preferably 0.01 to 0.1% by weight, and is generally used in an amount smaller than that of component (a). Component (c) is usually 0.1 to 5% by weight
It is used in the form of a concentrated aqueous solution. In carrying out the present invention, any chemicals commonly used in papermaking can be used as appropriate without special consideration. Other additive chemicals include relatively small amounts of aluminum sulfate (band), neutral papermaking dyes, sizing agents, and paper strength agents.
The yield of these additive chemicals themselves also increases, leading to a reduction in the amount added. [Example] The present invention will be specifically described below with reference to Examples.
However, the present invention is not limited in any way by the contents of the embodiments. All amounts of chemicals added are expressed in weight percent of the chemicals relative to the solid content of bone dry paper stock. Example 1 L-BKP (csf 300 ml) 3% pulp slurry was mixed with 0.5% aluminum sulfate (BAD), and as component (a), an acrylamide-based polymer having a cationic group (Himolok NR- 11L, Inc.
0.05% aqueous solution (manufactured by Kyoritsu Organic Industrial Research Institute), light calcium carbonate (Tama Pearl TP-121,
25% water suspension (manufactured by Okutama Kogyo Co., Ltd.) was added one by one while stirring. After diluting this paper stock with water to give a solid content concentration of 0.7%, a 0.3% aqueous dispersion of attapulgite (Atapulga clay DC-150, manufactured by Engelhart) was added as component (b), and then as component (c). Then, 0.03% CMC (Sunrose A50MC manufactured by Sanyo Kokusaku Pulp Co., Ltd.) aqueous solution was added with sufficient stirring to obtain a paper stock slurry with a pH of 8.5. The aqueous properties of the obtained stock slurry were measured. For the aqueous content, a Canadian Freeness Tester was used to measure the time required for the amount of liquid passing through the screen to reach 800 ml. In addition, the paper was made by hand using the TAPP1 standard sheet machine according to the conventional method.
The obtained wet paper was dehydrated by pressing at 3.5Kg/ cm2 pressure for 5 minutes, and then dried in a cylinder dryer (120℃±5℃).
It was dried. Humidity controlled at 20℃ and 65% humidity.
Bursting strength was measured using a MÃŒllen low-pressure tester in accordance with JISP8112. The texture of handmade paper was visually judged into four levels. In addition, the ash content was measured according to a conventional method, and the filler yield was calculated. Table 1 shows the above results.
Shown below. Comparative Example 1 shows the results when only two components were added.
Comparative Examples 1-D to 1-F show results when the order of addition of the three components was changed in A to 1-C. Example 2 [Acrylamide-based polymer (H・C-
Preparation of PAM)]. While cooling and stirring a polyacrylamide aqueous solution (polymer concentration 5%) with an average molecular weight of 500,000, drop an alkaline sodium hypochlorite aqueous solution and heat to 20℃.
After continuing the reaction for 1 hour, the pH was adjusted to 4.5 with dilute sulfuric acid to obtain an aqueous H.C-PAM solution. An aqueous suspension prepared by pre-mixing light calcium carbonate (same as in Example 1) and talc (ND Talc, manufactured by Nippon Talc Co., Ltd.) at a ratio of 2:1 as a filler was added to the same pulp slurry as used in Example 1. Add 25%, then add H・C-PAM aqueous solution as component (a).
0.05% was added with thorough stirring. This stock slurry was diluted with water so that the solid content concentration was 0.7%.
Furthermore, as component (b), 0.3% of sepiolite (Adeplus G, manufactured by Takeda Pharmaceutical Company Limited) aqueous dispersion,
Next, CMC (Sunrose F20HC,
A 0.04% aqueous solution (manufactured by Sanyo Kokusaku Pulp Co., Ltd.) was added to obtain a paper stock slurry with a pH of 8.3. This paper stock slurry was tested for water-based and handmade paper properties in the same manner as in Example 1, and the results are shown in Table 2. In addition, a comparative test was conducted according to Example 1. (Comparative Examples 2-A to 2-F) Example 3 [Acrylamide-based polymer (M・C-
Preparation of PAM)]. Predetermined amounts of formaldehyde and dimethylamine were added to a polyacrylamide aqueous solution (polymer concentration 5%) with an average molecular weight of 1 million, and the mixture was reacted at 60°C for 1.5 hours to obtain an M.C-PAM aqueous solution. To the same pulp slurry as used in Example 1, 0.15% of an emulsion of AKD (Harcon W, manufactured by Deitz Hercules Co., Ltd.) as a sizing agent was added with sufficient stirring. Next, as component (a), M・C-PAM aqueous solution 0.05%
After adding , the solid content concentration of paper stock slurry is
Diluted with water to 0.56%. Furthermore, the same light calcium carbonate aqueous suspension used in Example 1 was added as a filler so that the solid content concentration of the paper stock slurry was 0.7%, and then attapulgite (Atagel 50, manufactured by Engelhard) was added as component (b). Add 0.3% aqueous dispersion and then use CMC (Sunrose) as component (c).
F100LC, manufactured by Sanyo Kokusaku Pulp Co., Ltd.) aqueous solution
0.03 was added successively with stirring to obtain a stock slurry with a pH of 8.6. The obtained paper stock slurry was tested for its aqueous properties and handmade paper properties in the same manner as in Example 1, and the results are shown in Table 3. In addition, a comparative test was conducted according to Example 1. (Comparative example 3
-A~3-F)

【衚】【table】

【衚】【table】

〔䜜甚及び発明の効果〕[Action and effect of the invention]

本発明においお、各成分を所定の方法で組み合
わせた堎合の䜜甚に぀いおは次のように考えられ
る。 成分(a)ず成分(b)のみ添加した堎合には、歩留、
氎性ずも䞀応の効果は認められるが、その向䞊
は充分ではなく、又地合の悪化や玙力の䜎䞋も認
められる。これに察しお本発明の堎合には歩留、
氎性の向䞊の他に、地合及び玙力の改善が認め
られる。 これは耇鎖型構造を有する鉱物が有機物に察し
お倧きい吞着性を瀺すためず考えられる。 䟋えばアタパルゞダむトの耇雑な構造衚面䞊に
CMC―特にその糖鎖郚分―が吞着するこずによ
りアタパルゞダむト―CMCのコンプレツクスが
生成する。その結果、コンプレツクス䞭のカルボ
キシル基によ぀お、成分(a)で䞀次凝集したパルプ
や填料のフロツクが曎に匷く架橋するこずによ
り、比范的芏則的な構造を生成し、氎性及び地
合に良い結果を及がすず思われる。又、CMCは
氎溶性のためそのたたでは有効率が充分ではない
が、本発明のようにアタパルゞダむト等に吞着し
た状態で甚いるずその倧郚分が玙䞭に留たるた
め、玙力剀ずしおも効果を発揮しおいるものず考
えられる。 実斜䟋に瀺したように、本発明により䞭性抄玙
工皋においお充分に高い歩留及び氎性が埗られ
るず同時に、地合及び玙力に優れた䞭性抄玙が埗
られ、その工業的䟡倀は倧なるものである。
In the present invention, the effects when each component is combined in a predetermined manner are considered as follows. When only component (a) and component (b) are added, the yield,
Although some effects are observed with the water-based paper, the improvement is not sufficient, and deterioration of the formation and decrease in paper strength are also observed. On the other hand, in the case of the present invention, the yield,
In addition to improved water resistance, improvements in formation and paper strength were observed. This is thought to be because minerals with a double-chain structure exhibit a high adsorption ability for organic substances. For example, on the complex structure surface of attapulgiaite.
An attapulgite-CMC complex is formed by adsorption of CMC, especially its sugar chain moieties. As a result, the carboxyl groups in the complex cause the pulp and filler flocs that are primarily agglomerated in component (a) to be more strongly crosslinked, resulting in a relatively regular structure that is good for water and formation. It seems to have consequences. Also, since CMC is water-soluble, its effectiveness is not sufficient as it is, but when used in a state where it is adsorbed to attapulgite etc. as in the present invention, most of it remains in the paper, making it effective as a paper strength agent. It is thought that this is the case. As shown in the examples, the present invention allows a sufficiently high yield and aqueous property to be obtained in the neutral papermaking process, and at the same time, a neutral paper with excellent formation and paper strength can be obtained, and its industrial value is great. It is what it is.

Claims (1)

【特蚱請求の範囲】  填料を含むPH〜9.5のパルプスラリヌに (a) カチオン性基を有するアクリルアミド系ポリ
マヌ (b) 耇鎖型構造を有する鉱物質 (c) カルボキシメチルセルロヌス・ナトリりム塩 の぀の成分を(a)、(b)、(c)の順に添加した埌、抄
玙、也燥するこずを特城ずする䞭性抄玙方法。  填料が炭酞カルシりムである特蚱請求の範囲
第項蚘茉の䞭性抄玙方法。  カチオン性基を有するアクリルアミド系ポリ
マヌがポリアクリルアミドのホフマン分解物であ
る特蚱請求の範囲第項、第項蚘茉の䞭性抄玙
方法。  カチオン性基を有するアクリルアミド系ポリ
マヌがポリアクリルアミドのマンニツヒ反応物で
ある特蚱請求の範囲第項、第項蚘茉の䞭性抄
玙方法。  カチオン性基を有するアクリルアミド系ポリ
マヌがアクリルアミドずカチオン性モノマヌずの
共重合䜓である特蚱請求の範囲第項、第項蚘
茉の䞭性抄玙方法。  耇鎖型構造を有する鉱物質がアタパルゞダむ
トである特蚱請求の範囲第項ないし第項蚘茉
の䞭性抄玙方法。  耇鎖型構造を有する鉱物質がセピオラむトで
ある特蚱請求の範囲第項ないし第項蚘茉の䞭
性抄玙方法。  耇鎖型構造を有する鉱物質がパリゎルスカむ
トである特蚱請求の範囲第項ないし第項蚘茉
の䞭性抄玙方法。
[Claims] 1 Pulp slurry containing filler with a pH of 6 to 9.5 contains three components: (a) an acrylamide polymer having a cationic group, (b) a mineral substance having a double-chain structure, and (c) carboxymethylcellulose sodium salt. A neutral paper making method characterized by adding components (a), (b), and (c) in this order, followed by paper making and drying. 2. The neutral papermaking method according to claim 1, wherein the filler is calcium carbonate. 3. The neutral papermaking method according to claims 1 and 2, wherein the acrylamide-based polymer having a cationic group is a Hofmann decomposition product of polyacrylamide. 4. The neutral papermaking method according to claims 1 and 2, wherein the acrylamide-based polymer having a cationic group is a Mannitz reaction product of polyacrylamide. 5. The neutral papermaking method according to claims 1 and 2, wherein the acrylamide-based polymer having a cationic group is a copolymer of acrylamide and a cationic monomer. 6. The neutral papermaking method according to claims 1 to 5, wherein the mineral having a double-chain structure is attapulgite. 7. The neutral papermaking method according to claims 1 to 5, wherein the mineral having a double-chain structure is sepiolite. 8. The neutral papermaking method according to claims 1 to 5, wherein the mineral having a double-chain structure is palygorskite.
JP29064987A 1987-11-19 1987-11-19 Method for making neutral paper Granted JPH01132897A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP29064987A JPH01132897A (en) 1987-11-19 1987-11-19 Method for making neutral paper

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP29064987A JPH01132897A (en) 1987-11-19 1987-11-19 Method for making neutral paper

Publications (2)

Publication Number Publication Date
JPH01132897A JPH01132897A (en) 1989-05-25
JPH0160118B2 true JPH0160118B2 (en) 1989-12-21

Family

ID=17758702

Family Applications (1)

Application Number Title Priority Date Filing Date
JP29064987A Granted JPH01132897A (en) 1987-11-19 1987-11-19 Method for making neutral paper

Country Status (1)

Country Link
JP (1) JPH01132897A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102047719B1 (en) * 2019-05-22 2019-11-22 읎제혞 System for measuring water volume in reservoir

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3318176B2 (en) * 1995-11-24 2002-08-26 星光化孊工業株匏䌚瀟 Neutral paper manufacturing method
KR19990037728A (en) * 1996-06-21 1999-05-25 가부시킀가읎샀 바읎였 폎늬뚞 늬서치 How to Treat Bacterial Cellulose
ES2155320B1 (en) * 1998-02-16 2001-12-01 Guerrero Felix Canada A NEW COMPONENT OF THE PASTA FOR THE MANUFACTURE OF PAPER OR CARTON.
US8084139B2 (en) 2004-05-07 2011-12-27 Kao Corporation Article formed into sheet, method for producing the same and exothermic formed article

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102047719B1 (en) * 2019-05-22 2019-11-22 읎제혞 System for measuring water volume in reservoir

Also Published As

Publication number Publication date
JPH01132897A (en) 1989-05-25

Similar Documents

Publication Publication Date Title
US4643801A (en) Papermaking aid
KR100648569B1 (en) Cellulose Products comprising Silicate and Processes for preparing the Same
US4750974A (en) Papermaking aid
KR960015749B1 (en) A process for the production of cellulose fibre containing products in sheet or web form
FI114327B (en) Polysilicate microgels as retention / drainage agents in papermaking
JPS62156398A (en) Filled paper and its production
AU2002346464B2 (en) Modified starch and process therefor
SK6032000A3 (en) Modified starch composition for removing particles from aqueous dispersions
JP2003517421A (en) Metal silicate, cellulose product and method.
EP1025159A1 (en) Paper furnish containing modified starch
AU2002346464A1 (en) Modified starch and process therefor
JP2000506486A (en) Acid-resistant calcium carbonate composition and use thereof
JPH11513659A (en) Acid-resistant carbonate composition containing aluminum or magnesium hydroxide and use thereof
JPH0160118B2 (en)
KR20040068318A (en) Aqueous silica-containing composition and process for production of paper
PT700473E (en) PAPER PRODUCTION PROCESS
JPS6034698A (en) Paper sizing method
US8906201B2 (en) Use of acidic water in the manufacture of paper
EP1586704A1 (en) Use of ultrafine calcium carbonate particles in papermaking
RU2213822C1 (en) Printing paper manufacture method
WO2018053118A1 (en) Increased drainage performance in papermaking systems using microfibrillated cellulose
JP2001262498A (en) Pulp fiber, paper and method for producing paper
JPH0291298A (en) Neutral paper making
JP2751238B2 (en) Papermaking method